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Tolerability & Safety of Premarin Vaginal Cream in Indian Postmenopausal Women

A Postmarketing Surveillance Study Evaluating the Tolerability and Safety of PREMARIN VAGINAL CREAM in Indian Postmenopausal Women

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00484107
Enrollment
200
Registered
2007-06-08
Start date
2005-09-30
Completion date
2006-10-31
Last updated
2007-12-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postmenopause

Brief summary

This post-marketing study will provide local safety and tolerance data on the use of Premarin® vaginal cream.

Interventions

DRUGConjugated Estrogen Cream (Premarin®)

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients in whom Premarin vaginal cream is indicated. * In the opinion of the investigator, sufficient intelligence and motivation for the patient to continue throughout the study. * Provide signed informed consent.

Exclusion criteria

* Patients not willing to give informed consent.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026